JPH0478696B2 - - Google Patents
Info
- Publication number
- JPH0478696B2 JPH0478696B2 JP18292385A JP18292385A JPH0478696B2 JP H0478696 B2 JPH0478696 B2 JP H0478696B2 JP 18292385 A JP18292385 A JP 18292385A JP 18292385 A JP18292385 A JP 18292385A JP H0478696 B2 JPH0478696 B2 JP H0478696B2
- Authority
- JP
- Japan
- Prior art keywords
- aluminum alloy
- strength
- alloys
- rapid solidification
- hot
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910000838 Al alloy Inorganic materials 0.000 claims description 35
- 238000007712 rapid solidification Methods 0.000 claims description 28
- 238000001816 cooling Methods 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 13
- 229910052748 manganese Inorganic materials 0.000 claims description 11
- 229910052750 molybdenum Inorganic materials 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 3
- 229910045601 alloy Inorganic materials 0.000 description 37
- 239000000956 alloy Substances 0.000 description 37
- 238000000034 method Methods 0.000 description 29
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 17
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 16
- 239000011572 manganese Substances 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 238000000465 moulding Methods 0.000 description 8
- 239000006104 solid solution Substances 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 7
- 229910017052 cobalt Inorganic materials 0.000 description 7
- 239000010941 cobalt Substances 0.000 description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 7
- 239000011733 molybdenum Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 229910000765 intermetallic Inorganic materials 0.000 description 6
- 229910018131 Al-Mn Inorganic materials 0.000 description 5
- 229910018461 Al—Mn Inorganic materials 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 238000005979 thermal decomposition reaction Methods 0.000 description 5
- 229910001182 Mo alloy Inorganic materials 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000001192 hot extrusion Methods 0.000 description 4
- 229910018084 Al-Fe Inorganic materials 0.000 description 3
- 229910018192 Al—Fe Inorganic materials 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 238000009689 gas atomisation Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000010583 slow cooling Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000007725 thermal activation Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000009692 water atomization Methods 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
Description
〔発明の技術分野〕
この発明は、急冷凝固法により調製されたアル
ミニウム合金凝固体を熱間成形して、高強度の所
定形状のアルミニウム合金部材を製造するため
の、高強度アルミニウム合金部材の製造方法に関
するものである。
〔従来技術とその問題点〕
近年、急冷凝固法によつて製造された新種の合
金の各方面への応用が期待されている。急冷凝固
法によれば、従来困難とされていた、合金元素の
均一な固溶、過飽和固溶体の形成および金属間化
合物の微細分散化が可能となり、さらに、極微細
結晶組織や非晶質組織の合金が得られる場合もあ
るなど、合金の持つ特性を大幅に向上させること
ができる。
しかしながら、急冷凝固法は、一般に、溶融状
態の少量の合金を、多量の気体や液体の冷却媒体
に接触させるか、または、高速で移動する冷却さ
れた固体表面に流下させて急冷する方法であるか
ら、この方法によつて得られる凝固金属は、粉末
状、薄片状または薄肉リボン状のような微細形状
にならざるを得ない。
従つて、このようにして得られた微小形状の凝
固金属は、微小形状のまま使用する特殊用途のほ
かは、所定の大きさの部材に加工することが必要
とされる。例えば、急冷凝固法によつて製造され
た微細凝固体状のアルミニウム合金から、構造材
用の板材、棒材、形材などのアルミニウム合金部
材を製造するためには、一般に、微小凝固体状の
アルミニウム合金を集めそして圧縮することによ
り予備成形体を調製し、次いで、この予備成形体
に対し、圧延、押出し、鍜造などの展伸による成
形加工を施す成形加工工程が必要とされる。
上述した成形加工工程は、微小形状の凝固金属
同士の熱的活性化による強固な固着、および、成
形加工時の動力低減の観点から、熱間で行うこと
が好ましい。しかしながら、熱間で成形加工を行
なうと、急冷凝固によつて形成された好ましい非
平衡組織が、熱的活性化により平衡状態に復帰す
る結果、折角、急冷凝固によつて得られた特性の
大半が消失する問題がある。これは、急冷凝固に
よつて形成された過飽和固溶体が、低濃度の固溶
体と金属間化合物とに熱分解し、また、微晶質組
織が粗大化することによつて、急冷凝固組織が変
質するためである。
従来の溶解鋳造法によつて製造されるアルミニ
ウム合金の場合、Feなどの遷移金属元素の固溶
量は、平衡状態で約0.1wt.%であるが、急冷凝固
アルミニウム合金の場合は約10wt.%まで増加さ
れる。従つて、急冷凝固アルミニウム合金の粉末
や薄片では、ヴイツカース硬度が200以上を示す
ものが比較的容易に得られ、薄肉リボン状の急冷
凝固アルミニウム合金をそのまま引張り試験に供
すれば、50Kgf/mm2以上の引張り強さが示され
る。しかしながら、このような微小凝固体状の急
冷凝固アルミニウム合金に対し、熱間展伸加工を
含む成形加工を施して、所定形状の部材に成形し
た場合は、その部材のヴイツカース硬度は約100
に、そして、引張り強さは約30Kgf/mm2にまで低
下し、急冷凝固によつて得られた高硬度および高
強度特性が失われる。
このような硬度および強度の低下を防止するた
めに、成形加工を冷間で行うと、アルミニウム合
金に特有の強固な表面酸化皮膜が、微小凝固体間
の固着を妨げるので、良質な成形部材を得ること
ができない。そこで、上記成形加工を、200〜300
℃の温度のいわゆる温間で行えば、急冷凝固組織
の熱分解が比較的少なく、微小凝固体間の固着も
可能であるが、一方、成形のために大きな力を要
するため、得られる成形部材の寸法および形状が
限定され、且つ、成形のために特別な装置が必要
とされるので、実用的ではない。
〔発明の目的〕
従つて、この発明の目的は、急冷凝固法により
高密度アルミニウム合金部材を製造するに当り、
熱間で展伸加工を施しても強度の低下が生ずるこ
とがなく、急冷凝固によつて得られた優れた特性
が保持され、しかも、適度の延性を有する高強度
アルミニウム合金部材を製造するための方法を提
供することにある。
〔発明の概要〕
本発明者等は、急冷凝固法によつて、高強度ア
ルミニウム合金部材を製造するに当り、熱間で展
伸加工を施しても強度の低下が生ずることがな
く、急冷凝固によつて得られた優れた特性が保持
される方法を開発すべく鋭意研究を重ねた。
その結果、所定量のマンガンおよびモリブデン
を含有するアルミニウム合金は、急冷凝固によつ
てその硬度および強度が高められると共に、この
急冷凝固によつて得られた特性は、所定温度範囲
での熱間成形を行なつた場合に殆ど変化しないこ
と、および、上記アルミニウム合金において、マ
ンガンの一部を、鉄、ニツケルおよびコバルトの
少なくとも1つと置換すれば、熱間加工後の強度
が更に高まり、延性も改善されることを知見し
た。
この発明は、上記知見に基いてなされたもので
あつて、
Mo:4.0〜12wt.%、
Mo:0.2〜4.0wt.%、
および、必要に応じ、
Fe:0.1〜4.0wt.%、Ni:0.1〜4.0wt.%、
Co:0.1〜4.0wt.%からなる群から選んだ少な
くとも1つの元素で、その合計量が4.0wt.%以
下、
残り:アルミニウムおよび不可避不純物
からなる成分組成を有するアルミニウム合金を溶
製し、
次いで、前記アルミニウム合金を、103℃/sec
以上の冷却速度で急冷凝固して、粉末状または薄
片状の凝固体を調製し、
このようにして得られた凝固体を、そのまま、
または予備成形した上、少なくとも一度は500℃
以下の温度で熱間成形し、かくして、所定形状の
高強度を有するアルミニウム合金部材を製造する
ことに特徴を有するものである。
〔発明の構成〕
この発明において、アルミニウム合金の化学成
分組成範囲を上述のように限定した理由について
以下に述べる。
(1) マンガン(Mn)
マンガンは、鉄などと共に遷移金属元素であ
り、急冷凝固法によりアルミニウム中に過飽和に
固溶または微細に分散析出させると、強度が著し
く向上する作用を有している。また、熱拡散が遅
いので、Al−Mn合金は熱的安定性に優れ、約
300℃までの高温において高い強度を示す。Al−
Mn合金をAl−Fe合金と比較すると、Al−Mn合
金は、Al−Fe合金より低い冷却速度でも過飽和
固溶体が形成されやすく、融点が低いので溶解作
業が容易であり、高い弾性率が得られ、且つ、耐
食性も優れるなどAl−Fe合金よりも優れた性質
を有している。
マンガンの含有量が4.0wt.%未満では、上述し
た作用に所望の効果が得られず、一方、マンガン
の含有量が12wt.%を超えても上述した作用に格
別の向上が現われず、逆に金属間化合物の生成量
が多過ぎて延性が低下する問題が生ずる。従つ
て、マンガンの含有量は、4.0から12wt.%の範囲
内に限定すべきである。
(2) モリブデン(Mo)
Al−Mn合金は、上述した優れた特性を有して
いるが、急冷凝固後に行なわれる熱間成形加工に
おいて、熱分解により上記特性が大きく低下する
問題を有している。モリブデンは、Al−Mn合金
が持つ上記問題を解決するものであり、モリブデ
ンの添加によつて、急冷凝固の際に生ずる急冷凝
固組織の熱分解を緩慢にし、急冷凝固と熱間成形
加工との組合せによるアルミニウム合金部材の強
度を著しく向上させる作用を有している。
モリブデンの含有量が0.2wt.%未満では、上述
した作用に所望の効果が得られず、一方、モリブ
デンの含有量が4.0wt.%を超えると、金属間化合
物の生成量が多過ぎて延性が低下する問題が生ず
る。従つて、モリブデンの含有量は、0.2から
4.0wt.%の範囲内とすべきである。
(3) 鉄(Fe)、ニツケル(Ni)およびコバルト
(Co)
鉄、ニツケルおよびコバルトは、Al−Mn−
Mo合金の強度を向上させる作用を有しており、
強度向上の程度は、同量のマンガンよりもやや大
きい。更に、鉄、ニツケルおよびコバルトは、急
冷凝固と熱間成形加工との組合せによるアルミニ
ウム合金部材の延性を増大させる作用を有してい
る。従つて、Al−Mn−Mo合金において、マン
ガンの一部を、鉄、ニツケルおよびコバルトの少
なくとも1つに置換すると、強度の若干の向上に
加えて、引張り伸びを増加させることができる。
鉄、ニツケルおよびコバルトの少なくとも1つ
の含有量が0.1wt.%未満では、上述した作用に所
望の効果が得られず、一方、鉄、ニツケルおよび
コバルトの少なくとも1つの含有量またはその合
計含有量が4.0wt.%を超えると、金属間化合物の
生成量が多過ぎて、かえつて延性が低下する問題
が生ずる。従つて、鉄、ニツケルおよびコバルト
の少なくとも1つの含有量は、0.1から4.0wt.%の
範囲内とすべきであり、そして、これらの合計含
有量は、4.0wt.%以下とすべきである。
上述した成分組成範囲のAl−Mn−Mo合金は、
溶融状態からの急冷凝固によつて、高い強度特性
が発揮されるが、その冷却速度は103℃/sec以上
とすべきである。即ち、上記成分組成の溶製され
たアルミニウム合金を、103℃/sec以上の冷却速
度で急冷して得られた粉末状または薄片状の凝固
体を熱間成形することにより、従来の高強度アル
ミニウム合金に匹敵する室温強度と、従来合金を
上回る耐熱性および剛性を有する高強度アルミニ
ウム合金部材が得られる。
冷却速度103℃/sec未満では、合金元素が十分
に固溶せず、粗大な金属間化合物が析出するので
熱間成形加工によつて優れた強度および延性を有
する合金部材を得ることができない。なお、回転
ロール法などの手段により、105℃/sec以上の冷
却速度で急冷凝固された粉末、薄片を使用して
も、熱間成形加工された合金部材の強度は殆ど向
上せず、むしろ急冷凝固法の経済性が悪く、製造
費用の増大を招くことに注意すべきである。
通常のガス・アトマイズ法や水アトマイズ法に
よる冷却速度は、102〜104℃/secであり、改良
されたガス・アトマイズ法や回転ロール法による
冷却速度は、104〜106℃/secである。従つて、
急冷凝固手段は、上述した公知の方法によつて行
なうことができる。
上記のような条件による急冷凝固によつて得ら
れた粉末状、薄片状の凝固体、あるいは、薄肉リ
ボンを裁断した薄片状の微小凝固体、または、必
要に応じてより細かく粉砕した粉末を、そのま
ま、または予備成形した後、板材、棒材、形材
等、所要の形状に成形するための成形加工を、少
なくとも一度は熱間で行なうことが必要である。
このような熱間成形加工は、熱間プレス、熱間静
水圧プレス(HIP)、熱間圧延、熱間押出し、熱
間鍜造など公知の手段によつて行なうことができ
る。
熱間成形加工時の加工温度は、500℃以下とす
べきである。即ち、加工温度が500℃を超えると、
急冷凝固組織が急速に熱分解する結果、所望の強
度が得られない。好ましい温度範囲は350〜480℃
であつて、この温度範囲で成形加工を行えば、急
冷凝固組織の熱分解がほぼ抑制され、成形された
合金部材は、実用的に有意義な強度特性を示し、
且つ、一般に工業的に使用されている成形加工装
置の能力を超えることはない。
〔発明の実施例〕
実施例 1
第1表に示す成分組成の3種類の合金A,B,
Cを溶製した。合金AはMoを含有しないこの発
明の範囲外のAl−Mn合金であり、合金Bおよび
Cは、所定量のMoを含有するこの発明の範囲内
のAl−Mn−Mo合金である。
[Technical Field of the Invention] This invention relates to the production of high-strength aluminum alloy members for producing high-strength aluminum alloy members of a predetermined shape by hot forming aluminum alloy solidified bodies prepared by a rapid solidification method. It is about the method. [Prior art and its problems] In recent years, new types of alloys produced by the rapid solidification method are expected to be applied in various fields. The rapid solidification method enables the formation of uniform solid solutions of alloying elements, the formation of supersaturated solid solutions, and the fine dispersion of intermetallic compounds, which were previously considered difficult. In some cases, alloys can be obtained, and the properties of alloys can be greatly improved. However, the rapid solidification method generally involves rapidly cooling a small amount of a molten alloy by contacting it with a large amount of a gaseous or liquid cooling medium, or by causing it to flow down onto a rapidly moving cooled solid surface. Therefore, the solidified metal obtained by this method must have a fine shape such as powder, flake, or thin ribbon. Therefore, the finely shaped solidified metal thus obtained needs to be processed into a member of a predetermined size, except for special purposes in which it is used in its finely shaped form. For example, in order to manufacture aluminum alloy members such as plates, bars, and shapes for structural materials from a microsolidified aluminum alloy produced by the rapid solidification method, it is generally necessary to A forming process is required in which a preform is prepared by collecting and compressing an aluminum alloy, and then the preform is subjected to a forming process by stretching such as rolling, extrusion, and forging. The above-mentioned forming process is preferably carried out hot from the viewpoints of firm adhesion of micro-shaped solidified metals to each other through thermal activation and reduction of power during forming process. However, when hot forming is performed, the favorable nonequilibrium structure formed by rapid solidification returns to an equilibrium state through thermal activation, resulting in most of the properties obtained by rapid solidification. There is a problem that the data disappears. This is because the supersaturated solid solution formed by rapid solidification thermally decomposes into a low-concentration solid solution and an intermetallic compound, and the microcrystalline structure becomes coarser, causing the rapidly solidified structure to change in quality. It's for a reason. In the case of aluminum alloys manufactured by conventional melting and casting methods, the solid solution amount of transition metal elements such as Fe is approximately 0.1wt.% in an equilibrium state, but in the case of rapidly solidified aluminum alloys, it is approximately 10wt.%. %. Therefore, it is relatively easy to obtain rapidly solidified aluminum alloy powder or flakes with a Witzkars hardness of 200 or more, and if a thin ribbon-shaped rapidly solidified aluminum alloy is subjected to a tensile test as it is, it will have a hardness of 50 Kgf/mm 2 The above tensile strength is shown. However, when such a rapidly solidified aluminum alloy in the form of a microsolid is subjected to forming processing including hot stretching to form a member into a predetermined shape, the Witzkars hardness of the member is approximately 100.
Then, the tensile strength decreases to about 30 Kgf/mm 2 and the high hardness and high strength properties obtained by rapid solidification are lost. In order to prevent such a decrease in hardness and strength, if the forming process is performed cold, the strong surface oxide film unique to aluminum alloys will prevent the microsolids from adhering to each other, so it is necessary to use high-quality molded parts. can't get it. Therefore, the above molding process was performed for 200 to 300
If carried out at a so-called warm temperature of °C, there will be relatively little thermal decomposition of the rapidly solidified structure and it will be possible to bond between microsolids, but on the other hand, since a large force is required for forming, the resultant formed part will be It is not practical because it is limited in size and shape and requires special equipment for molding. [Object of the Invention] Therefore, the object of the present invention is to provide a method for producing high-density aluminum alloy members by the rapid solidification method.
To manufacture high-strength aluminum alloy members that do not lose strength even when subjected to hot drawing processing, maintain the excellent properties obtained by rapid solidification, and have appropriate ductility. The goal is to provide a method for [Summary of the Invention] The present inventors have discovered that when manufacturing high-strength aluminum alloy members using the rapid solidification method, there is no decrease in strength even when hot drawing is performed, and the rapid solidification process is effective. Intensive research has been carried out to develop a method that maintains the excellent properties obtained. As a result, the hardness and strength of aluminum alloys containing a certain amount of manganese and molybdenum are increased by rapid solidification, and the properties obtained by this rapid solidification are In addition, if part of the manganese in the above aluminum alloy is replaced with at least one of iron, nickel, and cobalt, the strength after hot working will further increase and the ductility will also improve. I found out that this happens. This invention was made based on the above findings, and includes Mo: 4.0 to 12 wt.%, Mo: 0.2 to 4.0 wt.%, and, if necessary, Fe: 0.1 to 4.0 wt.%, Ni: Aluminum with a composition consisting of at least one element selected from the group consisting of 0.1 to 4.0 wt.%, Co: 0.1 to 4.0 wt.%, the total amount of which is 4.0 wt.% or less, and the remainder: aluminum and inevitable impurities. An alloy is melted, and then the aluminum alloy is melted at 10 3 °C/sec.
Rapid solidification is performed at the above cooling rate to prepare a powdery or flaky solidified body, and the solidified body thus obtained is directly used as
or preformed and at least once at 500℃
The present invention is characterized in that it is hot-formed at a temperature below and thus produces an aluminum alloy member having a predetermined shape and high strength. [Structure of the Invention] In the present invention, the reason why the chemical composition range of the aluminum alloy is limited as described above will be described below. (1) Manganese (Mn) Manganese is a transition metal element along with iron, and when it is precipitated as a supersaturated solid solution or finely dispersed in aluminum using the rapid solidification method, it has the effect of significantly improving strength. In addition, because thermal diffusion is slow, Al-Mn alloys have excellent thermal stability and are approximately
Shows high strength at high temperatures up to 300℃. Al−
Comparing Mn alloys with Al-Fe alloys, Al-Mn alloys tend to form a supersaturated solid solution even at a lower cooling rate than Al-Fe alloys, and their lower melting points make melting easier, resulting in higher elastic modulus. In addition, it has better properties than Al-Fe alloys, such as excellent corrosion resistance. If the manganese content is less than 4.0wt.%, the desired effects described above cannot be obtained, while even if the manganese content exceeds 12wt.%, no particular improvement in the above-mentioned actions occurs, and vice versa. However, the problem arises that the amount of intermetallic compounds produced is too large, resulting in a decrease in ductility. Therefore, the manganese content should be limited within the range of 4.0 to 12 wt.%. (2) Molybdenum (Mo) Although Al-Mn alloy has the excellent properties mentioned above, it has the problem that the above properties are significantly reduced due to thermal decomposition during hot forming after rapid solidification. There is. Molybdenum solves the above-mentioned problems of Al-Mn alloys, and by adding molybdenum, the thermal decomposition of the rapidly solidified structure that occurs during rapid solidification is slowed down, and the process of rapid solidification and hot forming is improved. The combination has the effect of significantly improving the strength of the aluminum alloy member. If the content of molybdenum is less than 0.2wt.%, the desired effects described above cannot be obtained, while if the content of molybdenum exceeds 4.0wt.%, the amount of intermetallic compounds formed is too large, resulting in ductility. A problem arises in which the value decreases. Therefore, the content of molybdenum is from 0.2 to
It should be within the range of 4.0wt.%. (3) Iron (Fe), nickel (Ni) and cobalt (Co) Iron, nickel and cobalt are Al−Mn−
It has the effect of improving the strength of Mo alloy,
The degree of strength improvement is slightly greater than that of the same amount of manganese. Additionally, iron, nickel, and cobalt have the effect of increasing the ductility of aluminum alloy members through a combination of rapid solidification and hot forming. Therefore, replacing a portion of manganese with at least one of iron, nickel, and cobalt in an Al-Mn-Mo alloy can increase tensile elongation in addition to slightly improving strength. If the content of at least one of iron, nickel, and cobalt is less than 0.1 wt.%, the desired effect cannot be obtained in the above-mentioned action; If it exceeds 4.0 wt.%, the amount of intermetallic compounds produced will be too large, resulting in a problem that the ductility will be reduced. Therefore, the content of at least one of iron, nickel and cobalt should be in the range of 0.1 to 4.0 wt.%, and their total content should be no more than 4.0 wt.%. . The Al-Mn-Mo alloy with the above-mentioned composition range is
High strength properties are exhibited by rapid solidification from a molten state, but the cooling rate should be 10 3 °C/sec or higher. That is, by rapidly cooling a melted aluminum alloy having the above-mentioned composition at a cooling rate of 10 3 °C/sec or more and hot forming a powder or flake solidified body, it is possible to achieve the conventional high strength. A high-strength aluminum alloy member can be obtained that has room temperature strength comparable to that of aluminum alloys, and heat resistance and rigidity that exceed conventional alloys. If the cooling rate is less than 10 3 °C/sec, the alloying elements will not form a sufficient solid solution and coarse intermetallic compounds will precipitate, making it impossible to obtain an alloy member with excellent strength and ductility through hot forming. . Note that even if powder or flakes that have been rapidly solidified at a cooling rate of 10 5 °C/sec or more by means such as the rotating roll method are used, the strength of the hot-formed alloy member will hardly be improved; It should be noted that the rapid solidification method is not economical and increases manufacturing costs. The cooling rate with the normal gas atomization method or water atomization method is 10 2 to 10 4 °C/sec, and the cooling rate with the improved gas atomization method or rotating roll method is 10 4 to 10 6 °C/sec. It is. Therefore,
The rapid solidification can be carried out by the above-mentioned known method. A powdery or flaky solidified body obtained by rapid solidification under the above conditions, or a thin flaky microsolidified body obtained by cutting a thin ribbon, or a finely ground powder if necessary, As it is or after preforming, it is necessary to perform hot molding at least once to form it into a desired shape, such as a plate, bar, or profile.
Such hot forming processing can be performed by known means such as hot pressing, hot isostatic pressing (HIP), hot rolling, hot extrusion, and hot forging. The processing temperature during hot forming should be below 500°C. In other words, when the processing temperature exceeds 500℃,
As a result of rapid thermal decomposition of the rapidly solidified structure, the desired strength cannot be obtained. Preferred temperature range is 350-480℃
If the forming process is carried out in this temperature range, thermal decomposition of the rapidly solidified structure is almost suppressed, and the formed alloy member exhibits practically significant strength characteristics.
Moreover, it does not exceed the capabilities of molding equipment that is generally used industrially. [Embodiments of the invention] Example 1 Three types of alloys A, B, and
C was dissolved. Alloy A is an Al-Mn alloy outside the scope of this invention that does not contain Mo, and alloys B and C are Al-Mn-Mo alloys within the scope of this invention that contain a certain amount of Mo.
【表】
上記合金A,B,Cを各々再溶解し、その溶湯
に冷却媒体としてのアルゴンガスを吹き付けてア
トマイズし、アトマイズ条件の設定およびアトマ
イズ粉末の篩い分けにより、次の2種類の急冷凝
固粉末を調製した。
(1) 冷却速度:102〜103℃/sec未満
粒径:32〜100メツシユ(500〜150μm)
(2) 冷却速度:103〜105℃/sec
粒径:−100メツシユ(平均粒径約44μm)
上述の急冷凝固粉末を、400℃の温度で熱間プ
レスし、直径60mmのビレツトに予備成形した。次
いで上述のビレツトを、450から510℃の温度で、
押出し比25により熱間押出し成形し、直径12mmの
丸棒を製造した。
第2表は、このようにして製造した本発明合金
No.1〜4および比較合金No.1〜6の成分組成、熱
間押出しの際の押出し温度、および、室温での引
張り性質である。
比較合金No.1〜3は、冷却速度が本発明の範囲
を外れて遅く且つ比較合金No.1はその成分組成が
本発明の範囲外である。比較合金No.4はその成分
組成が本発明の範囲外である。そして、比較合金
No.5およびNo.6は、熱間押出しによる成形加工温
度が本発明の範囲を外れて高い。
上記第2表から明らかなように、本発明合金No.[Table] The above alloys A, B, and C are each remelted, and the molten metal is atomized by spraying argon gas as a cooling medium.The following two types of rapid solidification are achieved by setting the atomization conditions and sieving the atomized powder. A powder was prepared. (1) Cooling rate: less than 10 2 to 10 3 ℃/sec Particle size: 32 to 100 mesh (500 to 150 μm) (2) Cooling rate: 10 3 to 10 5 ℃/sec Particle size: -100 mesh (average particle (diameter: approximately 44 μm) The rapidly solidified powder described above was hot pressed at a temperature of 400° C. and preformed into a billet with a diameter of 60 mm. The billet described above is then heated at a temperature of 450 to 510°C.
Hot extrusion molding was performed at an extrusion ratio of 25 to produce a round bar with a diameter of 12 mm. Table 2 shows the alloys of the present invention produced in this way.
These are the component compositions of Nos. 1 to 4 and Comparative Alloys Nos. 1 to 6, extrusion temperature during hot extrusion, and tensile properties at room temperature. Comparative alloys Nos. 1 to 3 have slow cooling rates that are outside the scope of the present invention, and comparative alloy No. 1 has a component composition that is outside the scope of the present invention. Comparative alloy No. 4 has a composition outside the scope of the present invention. And comparison alloy
In No. 5 and No. 6, the molding temperature by hot extrusion is high and outside the range of the present invention. As is clear from Table 2 above, the invention alloy No.
【表】
1〜4は、引張り強さおよび伸びが共に優れてい
る。これに対して、比較合金No.1〜3は、冷却速
度が本発明の範囲を外れて遅いため、所望の強度
が得られず、特に比較合金No.1は成分組成も本発
明の範囲外のため特に強度が低い。比較合金No.4
は冷却速度および成形加工温度は本発明の範囲内
であるが、成分組成が本発明の範囲外であるため
強度が低い。そして、比較合金No.5および6は、
成形加工温度(押出し温度)が本発明の範囲を外
れて高いため、引張り強さおよび伸びが共に低
い。
実施例 2
第3表に示すように、本発明の範囲内の成分組
成を有する本発明合金No.5〜14および本発明の範
囲外の成分組成を有する比較合金No.7〜16を溶製
した。これらの合金を再溶解し、その溶湯を冷却
媒体としてのアルゴンガスの吹き付けによるアル
ゴンガス・アトマイズにより、急冷し凝固せし
め、ふるい分けして、−100メツシユの急冷凝固粉
末を調製した。その冷却温度は103〜105℃/sec
であつた。[Table] Samples 1 to 4 are excellent in both tensile strength and elongation. On the other hand, comparative alloys No. 1 to 3 have slow cooling rates that are outside the range of the present invention, so the desired strength cannot be obtained, and in particular, the composition of comparative alloy No. 1 is also outside the range of the present invention. Therefore, the strength is particularly low. Comparison alloy No.4
Although the cooling rate and molding temperature are within the range of the present invention, the strength is low because the component composition is outside the range of the present invention. Comparative alloys No. 5 and 6 are
Since the molding temperature (extrusion temperature) is high outside the range of the present invention, both tensile strength and elongation are low. Example 2 As shown in Table 3, inventive alloys Nos. 5 to 14 having compositions within the range of the present invention and comparative alloys Nos. 7 to 16 having compositions outside the range of the present invention were melt-produced. did. These alloys were remelted, the molten metal was rapidly cooled and solidified by argon gas atomization by spraying argon gas as a cooling medium, and sieved to prepare a -100 mesh rapidly solidified powder. Its cooling temperature is 10 3 to 10 5 ℃/sec
It was hot.
【表】【table】
以上詳述したように、この発明の方法によれ
ば、従来の高強度展伸用アルミニウム合金である
2000番台合金および7000番台合金に匹敵する室温
強度と、従来のアルミニウム合金に比べて極めて
高い高温強度を有し、しかも適度の伸びを有する
アルミニウム合金部材を製造することができ、且
つ、その製造は、従来の溶解鋳造材と熱間成形加
工によつて行なうことができるので、広範囲の応
用が可能である等、幾多の工業上優れた効果がも
たらされる。
As detailed above, according to the method of the present invention, conventional high-strength aluminum alloys for drawing can be
It is possible to manufacture aluminum alloy members that have room temperature strength comparable to 2000 series alloys and 7000 series alloys, extremely high high temperature strength compared to conventional aluminum alloys, and moderate elongation. Since this process can be carried out using conventional melt-casting materials and hot forming, it can be applied in a wide range of applications and brings about many excellent industrial effects.
Claims (1)
製し、 次いで、前記アルミニウム合金を、103℃/sec
以上の冷却速度で急冷凝固して、粉末状または薄
片状の凝固体を調製し、 このようにして得られた凝固体を、そのまま、
または予備成形した上、少なくとも一度は500℃
以下の温度で熱間成形し、かくして、所定形状の
高強度を有するアルミニウム合金部材を製造する
ことを特徴とする高強度アルミニウム合金部材の
製造方法。 2 Mn:4.0〜12wt.%、 Mo:0.2〜4.0wt.%、 および、 Fe:0.1〜4.0wt.%、Ni:0.1〜4.0wt.%、 Co:0.1〜4.0wt.%からなる群から選んだ少な
くとも1つの元素で、その合計量が4.0wt.%以
下、 残り:アルミニウムおよび不可避不純物 からなる成分組成を有するアルミニウム合金を溶
製し、 次いで、前記アルミニウム合金を、103/sec以
上の冷却速度で急冷凝固して、粉末状または薄片
状の凝固体を調製し、 このようにして得られた凝固体を、そのまま、
または予備成形した上、少なくとも一度は500℃
以上の温度で熱間成形し、かくして、所定形状の
高強度を有するアルミニウム合金部材を製造する
ことを特徴とする高強度アルミニウム合金部材の
製造方法。[Claims] 1. An aluminum alloy having a composition consisting of Mn: 4.0 to 12 wt.%, Mo: 0.2 to 4.0 wt.%, and the remainder: aluminum and unavoidable impurities is melted, and then the aluminum alloy is 10 3 ℃/sec
Rapid solidification is performed at the above cooling rate to prepare a powdery or flaky solidified body, and the solidified body thus obtained is directly used as
or preformed and at least once at 500℃
1. A method for producing a high-strength aluminum alloy member, which comprises hot forming at a temperature of: 2 From the group consisting of Mn: 4.0 to 12 wt.%, Mo: 0.2 to 4.0 wt.%, Fe: 0.1 to 4.0 wt.%, Ni: 0.1 to 4.0 wt.%, Co: 0.1 to 4.0 wt.% An aluminum alloy having a composition of at least one selected element with a total content of 4.0 wt.% or less, the remainder: aluminum and unavoidable impurities is melted, and then the aluminum alloy is heated at a rate of 10 3 /sec or more. Rapid solidification is performed at a cooling rate to prepare a powdery or flaky solidified body, and the solidified body thus obtained is directly used as is.
or preformed and at least once at 500℃
A method for producing a high-strength aluminum alloy member, which comprises hot forming at a temperature above, thereby producing an aluminum alloy member having a predetermined shape and high strength.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18292385A JPS6244539A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18292385A JPS6244539A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6244539A JPS6244539A (en) | 1987-02-26 |
| JPH0478696B2 true JPH0478696B2 (en) | 1992-12-11 |
Family
ID=16126737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18292385A Granted JPS6244539A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6244539A (en) |
-
1985
- 1985-08-22 JP JP18292385A patent/JPS6244539A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6244539A (en) | 1987-02-26 |
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